Linked Data
MyVariant Identifiers:
chr10:g.112333499T>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.110573741T>C , CM000672.2:g.110573741T>C | GRCh38 |
| NC_000010.10:g.112333499T>C , CM000672.1:g.112333499T>C | GRCh37 |
| NC_000010.9:g.112323489T>C | NCBI36 |
| NG_012217.1:g.11051T>C , LRG_774:g.11051T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000684988.1:n.259T>C | ||
| ENST00000687823.1:n.45-1595T>C | ||
| ENST00000689932.1:n.599T>C | ||
| ENST00000691297.1:n.259T>C | ||
| ENST00000691527.1:n.216T>C | ||
| ENST00000692792.1:n.245T>C | ||
| ENST00000361804.5:c.126T>C MANE Select | ENSP00000354720.5:p.Phe42= | |
| ENST00000361804.4:c.126T>C | ENSP00000354720.4:p.Phe42= | |
| ENST00000462899.1:n.272T>C | ||
| NM_005445.3:c.126T>C , LRG_774t1:c.126T>C | NP_005436.1:p.Phe42= | |
| NM_005445.4:c.126T>C MANE Select | NP_005436.1:p.Phe42= |